Method for preparing polyurethane function material with surface modified by polyvinyl pyrrolidone
A technology of polyvinylpyrrolidone and functional materials, which is applied in the field of preparation of hydrophilic coatings, can solve problems such as easy peeling off of coatings, failure to apply and popularize, etc., achieves the effect of simple production process and improved surface hydrophilicity
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Embodiment 1
[0033] 1) Preparation of polyvinylpyrrolidone (Init-PVP-N 3 ): first purify N-vinylpyrrolidone by vacuum distillation to remove the polymerization inhibitor. Under nitrogen protection, 0.135g (0.94mmol) cuprous bromide (CuBr) 0.39mL (1.88mmol) N, N, N', N", N"'-pentamethyldiethylenetriamine (PMDETA ) and 10mL (0.094mol) of N-vinylpyrrolidone were added to a 50mL three-neck round bottom flask equipped with a reflux condenser, and continuously stirred with a magnetic stirrer, and then the initiator 2-bromoisobutyric acid (1.57 g, 0.0094mol), heated to 90°C and refluxed for 72 hours. After the reaction, cool to room temperature, pour the reaction mixture in the flask into a 100mL acetic acid solution, filter, and rinse with excess deionized water successively, and vacuum dry to obtain polyvinylpyrrolidone (Init- PVP-Br). Take 0.130g (~0.04mmol) of bromine-terminated polyvinylpyrrolidone (Init-PVP-Br) obtained above and 0.163g (2.50mmol) of sodium azide (NaN 3 ) was dissolved ...
Embodiment 2
[0037] 1) Preparation of polyvinylpyrrolidone (Init-PVP-N3 ): first purify N-vinylpyrrolidone by vacuum distillation to remove the polymerization inhibitor. Under nitrogen protection, 0.135g (0.94mmol) cuprous bromide (CuBr) 0.39mL (1.88mmol) N, N, N', N", N"'-pentamethyldiethylenetriamine (PMDETA ) and 10mL (0.094mol) of N-vinylpyrrolidone were added to a 50mL three-neck round bottom flask equipped with a reflux condenser, and continuously stirred with a magnetic stirrer, and then the initiator 2-bromoisobutyric acid (1.57 g, 0.0094mol), heated to 90°C and refluxed for 72 hours. After the reaction, cool to room temperature, pour the reaction mixture in the flask into a 100mL acetic acid solution, filter, and rinse with excess deionized water successively, and vacuum dry to obtain polyvinylpyrrolidone (Init- PVP-Br). Take 0.130g (~0.04mmol) of bromine-terminated polyvinylpyrrolidone (Init-PVP-Br) obtained above and 0.163g (2.50mmol) of sodium azide (NaN 3 ) was dissolved in...
Embodiment 3
[0041] 1) Preparation of polyvinylpyrrolidone (Init-PVP-N 3 ): first purify N-vinylpyrrolidone by vacuum distillation to remove the polymerization inhibitor. Under nitrogen protection, 0.135g (0.94mmol) cuprous bromide (CuBr) 0.39mL (1.88mmol) N, N, N', N", N"'-pentamethyldiethylenetriamine (PMDETA ) and 10mL (0.094mol) of N-vinylpyrrolidone were added to a 50mL three-neck round bottom flask equipped with a reflux condenser, and continuously stirred with a magnetic stirrer, and then the initiator 2-bromoisobutyric acid (1.57 g, 0.0094mol), heated to 90°C and refluxed for 72 hours. After the reaction, cool to room temperature, pour the reaction mixture in the flask into a 100mL acetic acid solution, filter, and rinse with excess deionized water successively, and vacuum dry to obtain polyvinylpyrrolidone (Init- PVP-Br). Take 0.130g (~0.04mmol) of bromine-terminated polyvinylpyrrolidone (Init-PVP-Br) obtained above and 0.163g (2.50mmol) of sodium azide (NaN 3 ) was dissolved ...
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